Your search returned 571 results.

Results
	421.	A method for the quantitation of conjugated bile acids in dried blood spots using electrospray ionization-mass spectrometry. [electronic resource] by Mills, K A Mushtaq, I Johnson, A W Whitfield, P D Clayton, P T Producer: 19980501 In: Pediatric research vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	422.	[Phenotype--genotype relationships in peroxisome biogenesis disorders]. [electronic resource] by Shimozawa, N Producer: 20010726 In: No to shinkei = Brain and nerve vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	423.	Peroxisomal acyl-CoA-oxidase deficiency: two new cases. [electronic resource] by Carrozzo, Rosalba Bellini, Carlo Lucioli, Simona Deodato, Federica Cassandrini, Denise Cassanello, Michela Caruso, Ubaldo Rizzo, Cristiano Rizza, Teresa Napolitano, Matteo L Wanders, Ronald J A Jakobs, Cornelis Bruno, Claudio Santorelli, Filippo M Dionisi-Vici, Carlo Bonioli, Eugenio Producer: 20080820 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	424.	[Molecular mechanisms of peroxisome biogenesis in yeasts]. [electronic resource] by Sibirnyĭ, A A Producer: 20120731 In: Molekuliarnaia biologiia vol. 46 Availability: No items available. Save to lists Add to cart (remove)
	425.	Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency. [electronic resource] by Ferdinandusse, S Overmars, H Denis, S Waterham, H R Wanders, R J Vreken, P Producer: 20010628 In: Journal of lipid research vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	426.	Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1. [electronic resource] by Imamura, A Shimozawa, N Suzuki, Y Zhang, Z Tsukamoto, T Fujiki, Y Orii, T Osumi, T Wanders, R J Kondo, N Producer: 20001019 In: Pediatric research vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	427.	Approaches to studies on peroxisome biogenesis and human peroxisome-deficient disorders. [electronic resource] by Fujiki, Y Producer: 19970210 In: Annals of the New York Academy of Sciences vol. 804 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	428.	The identification of unusual bile acid metabolites by tandem mass spectrometry: use of low-energy collision-induced dissociation to produce informative spectra. [electronic resource] by Lemonde, H A Johnson, A W Clayton, P T Producer: 19990721 In: Rapid communications in mass spectrometry : RCM vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	429.	Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a case. [electronic resource] by Akaboshi, S Tomita, Y Suzuki, Y Une, M Sohma, O Takashima, S Takeshita, K Producer: 19970728 In: Brain & development vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	430.	Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature. [electronic resource] by Taylor, Rachel L Handley, Mark T Waller, Sarah Campbell, Christopher Urquhart, Jill Meynert, Alison M Ellingford, Jamie M Donnelly, Deirdre Wilcox, Gisela Lloyd, I Chris Mundy, Helen FitzPatrick, David R Deshpande, Charu Clayton-Smith, Jill Black, Graeme C Producer: 20170623 In: Investigative ophthalmology & visual science vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	431.	Proton MR spectroscopy of childhood adrenoleukodystrophy. [electronic resource] by Rajanayagam, V Grad, J Krivit, W Loes, D J Lockman, L Shapiro, E Balthazor, M Aeppli, D Stillman, A E Producer: 19961204 In: AJNR. American journal of neuroradiology vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	432.	Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders. [electronic resource] by Chang, C C Lee, W H Moser, H Valle, D Gould, S J Producer: 19970425 In: Nature genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	433.	Inborn Errors of Metabolism (Metabolic Disorders). [electronic resource] by Rice, Gregory M Steiner, Robert D Producer: 20170213 In: Pediatrics in review vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	434.	Peroxisomal disorders: overview. [electronic resource] by Moser, H W Moser, A B Producer: 19970210 In: Annals of the New York Academy of Sciences vol. 804 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	435.	X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy. [electronic resource] by van Geel, B M Assies, J Wanders, R J Barth, P G Producer: 19970724 In: Journal of neurology, neurosurgery, and psychiatry vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	436.	Peroxisomal proliferator-activated ligand therapy for HIV lipodystrophy. [electronic resource] by Smith, K J Skelton, H G Producer: 20010531 In: Clinical and experimental dermatology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	437.	Temperature sensitive acyl-CoA oxidase import in group A peroxisome biogenesis disorders. [electronic resource] by Imamura, A Shimozawa, N Suzuki, Y Zhang, Z Tsukamoto, T Orii, T Osumi, T Kondo, N Producer: 20020307 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	438.	Microglia: the effector cell for reconstitution of the central nervous system following bone marrow transplantation for lysosomal and peroxisomal storage diseases. [electronic resource] by Krivit, W Sung, J H Shapiro, E G Lockman, L A Producer: 19951215 In: Cell transplantation vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	439.	Peroxisomal deficiencies are associated with altered activity of endothelial NOS in human fibroblasts. [electronic resource] by Koeck, T Kremser, K Producer: 20010809 In: Nitric oxide : biology and chemistry vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	440.	Cholesterol metabolism in cells with different peroxisomal defects. [electronic resource] by Oettl, K Malle, E Grillhofer, H Sattler, W Kostner, G M Producer: 19961127 In: Clinica chimica acta; international journal of clinical chemistry vol. 251 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 571 results.